Temi Santa, Rudyk Christopher, Armstrong Jennifer, Landrigan Jeffrey A, Dedek Chris, Salmaso Natalina, Hildebrand Michael E
Department of Neuroscience, Carleton University , Ottawa, Canada.
Neuroscience Program, Ottawa Hospital Research Institute , Ottawa, ON, Canada.
Channels (Austin). 2021 Dec;15(1):179-192. doi: 10.1080/19336950.2020.1871205.
N-methyl-D-aspartate receptors (NMDARs) are excitatory ionotropic glutamate receptors expressed throughout the CNS, including in the spinal dorsal horn. The GluN2 subtypes of NMDAR subunit, which include GluN2A, GluN2B, and GluN2D in the dorsal horn, confer NMDARs with structural and functional variability, enabling heterogeneity in synaptic transmission and plasticity. Despite essential roles for NMDARs in physiological and pathological pain processing, the distribution and function of these specific GluN2 isoforms across dorsal horn laminae remain poorly understood. Surprisingly, there is a complete lack of knowledge of GluN2 expression in female rodents. We, therefore, investigated the relative expression of specific GluN2 variants in the dorsal horn of lumbar (L4/L5) spinal cord from both male and female rats. In order to detect synaptic GluN2 isoforms, we used pepsin antigen-retrieval to unmask these highly cross-linked protein complexes. We found that GluN2B and GluN2D are preferentially localized to the pain-processing superficial regions of the dorsal horn in males, while only GluN2B is predominantly localized to the superficial dorsal horn of female rats. The GluN2A subunit is diffusely localized to neuropil throughout the dorsal horn of both males and females, while GluN2B and GluN2D immunolabelling are found both in the neuropil and on the soma of dorsal horn neurons. Finally, we identified an unexpected enhanced expression of GluN2B in the medial division of the superficial dorsal horn, but in males only. These sex-specific localization patterns of GluN2-NMDAR subunits across dorsal horn laminae have significant implications for the understanding of divergent spinal mechanisms of pain processing.
N-甲基-D-天冬氨酸受体(NMDARs)是兴奋性离子型谷氨酸受体,在整个中枢神经系统中均有表达,包括脊髓背角。NMDAR亚基的GluN2亚型,在背角中包括GluN2A、GluN2B和GluN2D,赋予NMDARs结构和功能的变异性,使得突触传递和可塑性具有异质性。尽管NMDARs在生理和病理性疼痛处理中发挥着重要作用,但这些特定的GluN2亚型在背角板层中的分布和功能仍知之甚少。令人惊讶的是,对于雌性啮齿动物中GluN2的表达完全缺乏了解。因此,我们研究了雄性和雌性大鼠腰段(L4/L5)脊髓背角中特定GluN2变体的相对表达。为了检测突触GluN2亚型,我们使用胃蛋白酶抗原修复来解开这些高度交联的蛋白质复合物。我们发现,GluN2B和GluN2D优先定位于雄性背角的疼痛处理浅表区域,而在雌性大鼠中,只有GluN2B主要定位于背角浅表区域。GluN2A亚基广泛分布于雄性和雌性背角的神经毡中,而GluN2B和GluN2D免疫标记则在神经毡和背角神经元的胞体中均有发现。最后,我们发现仅在雄性中,GluN2B在浅表背角内侧部意外地增强表达。GluN2-NMDAR亚基在背角板层中的这些性别特异性定位模式,对于理解不同的脊髓疼痛处理机制具有重要意义。